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Journal of Inherited Metabolic Disease

Volumn 15, Issue 2, 1992, Pages 161-170

DNA-based presymptomatic diagnosis of Wilson disease

(7) Gaffney, D a Walker, J L a O'Donnell, J G a Fell, G S a O'Neill, K F b Park, R H R a Russell, R I a

a GLASGOW ROYAL INFIRMARY (United Kingdom)

b Midlock Medical Centre (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

COPPER;

ARTICLE; CHROMOSOME 13; CLINICAL ARTICLE; COPPER METABOLISM; FEMALE; HUMAN; LIVER BIOPSY; MALE; PEDIGREE ANALYSIS; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SCHOOL CHILD; WILSON DISEASE;

CHROMOSOMES, HUMAN, PAIR 13; DNA; FEMALE; GENETIC MARKERS; HAPLOTYPES; HEPATOLENTICULAR DEGENERATION; HETEROZYGOTE DETECTION; HUMAN; MALE; PEDIGREE; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; SUPPORT, NON-U.S. GOV'T;

EID: 0026550373 PISSN: 01418955 EISSN: 15732665 Source Type: Journal
DOI: 10.1007/BF01799625 Document Type: Article

Times cited : (8)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.